rs2033211003 Rat Genome Database

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Variant: rs2033211003 -  Homo sapiens

RGD ID: 28905679
RS ID: rs2033211003
ClinVar ID: CV877960
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRIM37  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 57,075,678
GRCh38 17 58,998,317
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009298.1:g.113589C>G
NC_000017.11:g.58998317G>C
NC_000017.10:g.57075678G>C
NR_148347.2:n.4313C>G
More... 		01/13/2018 3 prime utr variant uncertain significance Muscle-liver-brain-eye nanism; Perheentupa syndrome; Pericardial constriction and growth failure
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TRIM37
Accession:NM_015294
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001320987
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001320988
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001320990
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_017024670
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_017024669
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001353085
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001353082
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001353086
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001353084
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NM_001353083
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_047436125
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_047436124
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_047436126
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_047436120
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:XM_047436119
Location:3UTRS;EXON

Gene Symbol:TRIM37
Accession:NR_148347
Location:EXON;NON-CODING

Gene Symbol:TRIM37
Accession:NR_148346
Location:EXON;NON-CODING

Gene Symbol:TRIM37
Accession:NM_001005207
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_005257385
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524833
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524836
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524832
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524831
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_011524834
Location:INTRON

Gene Symbol:TRIM37
Accession:NM_001320989
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024663
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024662
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024667
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024665
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_017024673
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436110
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436107
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436111
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436122
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436121
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436114
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436113
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436117
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436108
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436123
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436116
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436115
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436106
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436109
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436112
Location:INTRON

Gene Symbol:TRIM37
Accession:XM_047436118
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001126651 CLINVAR
dbSNP (RS) rs2033211003 CLINVAR
MedGen C0524582 CLINVAR
NCBI Gene TRIM37 CLINVAR
OMIM 253250 CLINVAR
  605073 CLINVAR
SNOMED CT 81604003 CLINVAR